Ketone/Aldehyde → Amine via Reductive Amination (Planning Page): Workflow + Practice

Reductive amination is the most direct way to convert carbonyls to amines: form an imine/iminium, then reduce it selectively.

  • Reaction: Ketone/Aldehyde → Amine via Reductive Amination (Planning Page)
  • What it does: Reductive amination is the most direct way to convert carbonyls to amines: form an imine/iminium, then reduce it selectively.
  • Typical reagents: NaBH3CN, AcOH (or NaBH(OAc)3)
  • Key intermediate: Iminium ion
  • Driving force: Hydride delivery to electrophile
  • Exam type: Choose reagents
  • Exam type: Plan order of operations
  • Exam type: Chemoselectivity

Related Resources

All 194 Mechanisms — Synthesis Strategy & Problem Solving Mechanism Flashcards AI Reaction Predictor Ask the AI Tutor